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MXP Start Up Kit

FDA UDI

Class I (US FDA UDI)

by Thermogenesis Corp.

Identity

Trade Name
MXP Start Up Kit FDA UDI
Generic Name
Haematological concentrate system preparation kit, bone marrow concentration FDA UDI
Device Name
Startup kit for the MXP System FDA UDI
Model / Reference
8-5142 FDA UDI
Description
Startup kit for the MXP System FDA UDI

Identifiers

Catalog Number
8-5142 FDA UDI
Primary DI / UDI-DI
00886368000391 FDA UDI
FDA Product Code
JQC FDA UDI
GMDN Term
Haematological concentrate system preparation kit, bone marrow concentration FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological concentrate system preparation kit, bone marrow concentration

MXP Start Up Kit by Thermogenesis Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological concentrate system preparation kit, bone marrow concentration.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermogenesis Corp.

Sources (1)

  • FDA UDI 77e45b44-e7b4-4382-a66e-44131c85aa15 35 fields · synced May 30, 2026